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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DAROLUTAMIDE Cause Product use issue? 27 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product use issue have been filed in association with DAROLUTAMIDE (NUBEQA). This represents 0.8% of all adverse event reports for DAROLUTAMIDE.

27
Reports of Product use issue with DAROLUTAMIDE
0.8%
of all DAROLUTAMIDE reports
3
Deaths
5
Hospitalizations

How Dangerous Is Product use issue From DAROLUTAMIDE?

Of the 27 reports, 3 (11.1%) resulted in death, 5 (18.5%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DAROLUTAMIDE. However, 27 reports have been filed with the FAERS database.

What Other Side Effects Does DAROLUTAMIDE Cause?

Fatigue (384) Death (361) Hot flush (203) Asthenia (173) Prostatic specific antigen increased (156) Off label use (133) Neuropathy peripheral (127) Diarrhoea (122) Dizziness (122) Rash (116)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which DAROLUTAMIDE Alternatives Have Lower Product use issue Risk?

DAROLUTAMIDE vs DARUNAVIR DAROLUTAMIDE vs DARUNAVIR ETHANOLATE DAROLUTAMIDE vs DARUNAVIR\RITONAVIR DAROLUTAMIDE vs DASABUVIR DAROLUTAMIDE vs DASABUVIR\OMBITASVIR HEMINONAHYDRATE\PARITAPREVIR\RITONAVIR

Related Pages

DAROLUTAMIDE Full Profile All Product use issue Reports All Drugs Causing Product use issue DAROLUTAMIDE Demographics